Lack of effects of eight-week left dorsolateral prefrontal theta burst stimulation on white matter macro/microstructure and connection in autism

• Published in: Brain imaging and behavior 2024-08, Vol.18 (4), p.794-807
• Main Authors: Yeh, Chun-Hung, Lin, Po-Chun, Tseng, Rung-Yu, Chao, Yi-Ping, Wu, Chen-Te, Chou, Tai-Li, Chen, Rou-Shayn, Gau, Susan Shur-Fen, Ni, Hsing-Chang, Lin, Hsiang-Yuan
• Format: Article
• Language: English
• Subjects: Achievement tests; Adolescent; Adult; Adults; Angular resolution; Autism; Autistic Disorder - diagnostic imaging; Autistic Disorder - physiopathology; Biomedical and Life Sciences; Biomedicine; Brain; Child; Children; Diffusion Magnetic Resonance Imaging - methods; Diffusion rate; Dorsolateral Prefrontal Cortex - diagnostic imaging; Double-Blind Method; Female; Humans; Magnetic resonance imaging; Male; Medical imaging; Microstructure; Neural Pathways - physiopathology; Neuroimaging; Neuropsychology; Neuroradiology; Neurosciences; Prefrontal cortex; Prefrontal Cortex - diagnostic imaging; Prefrontal Cortex - physiopathology; Psychiatry; Statistical analysis; Stimulation; Substantia alba; Transcranial Magnetic Stimulation - methods; White Matter - diagnostic imaging; Young Adult
• ISSN: 1931-7565; 1931-7557; 1931-7565
• DOI: 10.1007/s11682-024-00874-x

Whether brain stimulation could modulate brain structure in autism remains unknown. This study explored the impact of continuous theta burst stimulation (cTBS) over the left dorsolateral prefrontal cortex (DLPFC) on white matter macro/microstructure in intellectually able children and emerging adults with autism. Sixty autistic participants were randomized (30 active) and received active or sham cTBS for eight weeks twice per week, 16 total sessions using a double-blind (participant-, rater-, analyst-blinded) design. All participants received high-angular resolution diffusion MR imaging at baseline and week 8. Twenty-eight participants in the active group and twenty-seven in the sham group with good imaging quality entered the final analysis. With longitudinal fixel-based analysis and network-based statistics, we found no significant difference between the active and sham groups in changes of white matter macro/microstructure and connections following cTBS. In addition, we found no association between baseline white matter macro/microstructure and autistic symptom changes from baseline to week 8 in the active group. In conclusion, we did not find a significant impact of left DLPFC cTBS on white matter macro/microstructure and connections in children and emerging adults with autism. These findings need to be interpreted in the context that the current intellectually able cohort in a single university hospital site limits the generalizability. Future studies are required to investigate if higher stimulation intensities and/or doses, other personal factors, or rTMS parameters might confer significant brain structural changes visible on MRI in ASD.